Job Details

Job Summary:

Just Pharma are currently working on behalf of various leading organisations in the pharmaceutical industry looking for experienced Drug Safety Professionals with experience of Case Management. The positions are available office based at various levels of seniority and come with a very competitive salary and benefits packages.

Requirements:

The successful candidate will be required to:

• Preparation and revision of department SOPs and WPDs as well as preparing for and attending audits.
• Contributing to the ongoing enhancement of Pharmacovigilance processes and writing Standard Operating Procedures.
• Maintain knowledge and understanding of SOPs and WPDs; current global regulations and ICH/local guidelines regarding clinical trials, regulatory documents and safety issues
• Effectively interface with project teams, client company, and investigators regarding SAE activities

The ideal candidate will have:

• Candidates should have a Life Sciences qualification or be a licensed health care professional.
• Previous PVG/drug safety experience is essential within a pharmaceutical, clinical or healthcare setting
• Competent with medical terminology, excellent communication abilities and possess good IT skills
• Contributing to the ongoing enhancement of Pharmacovigilance processes and writing Standard Operating Procedures.

For further information on this position or to have a confidential conversation please contact me on 0044 1707 226502 or E-mail at James@Justpharma.co.uk

Key Skills,
Drug Safety, Drug Safety Associate, DSA, Pharmacovigilance, Pharmacovigilance Associate, Pharmacovigilance Senior Associate, Principle Pharmacovigilance Associate, Case Management, Case Processing, England, South East, Hertfordshire, Cambridgeshire, Bedfordshire, Suffolk, Essex, United Kingdom, UK.